Cite
HARVARD Citation
Khan, R. et al. (2020). A founder RDH5 splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindreds. Ophthalmic genetics. pp. 7-12. [Online].
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Khan, R. et al. (2020). A founder RDH5 splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindreds. Ophthalmic genetics. pp. 7-12. [Online].